Haemopharm Biofluids S.r.l.
ItalyFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
HMB32 Dialysis Solution Ref K212052
Regimes: 510(k) Registry: 510(k)HMB32 Ref K150966
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Haemopharm Biofluids S.R.L. have in the registry?
The registry currently lists 2 devices for Haemopharm Biofluids S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Haemopharm Biofluids S.R.L.'s devices?
Among its 2 most recently registered devices, Haemopharm Biofluids S.R.L. has devices listed in FDA 510(k) (2 devices).
What risk classes do Haemopharm Biofluids S.R.L.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Haemopharm Biofluids S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Haemopharm Biofluids S.R.L. in the registry?
The most recently registered devices listed for Haemopharm Biofluids S.R.L. include HMB32 Dialysis Solution and HMB32.